Calceolarioside B inhibits SARS-CoV-2 Omicron BA.2 variant cell entry and modulates immune response

  • Virol J. 2024 Dec 21;21(1):329. doi: 10.1186/s12985-024-02566-w.
Xiao-Bin Lin  #  1 Yu-Zhi Yao  #  1  2 Qi-Rong Wen  3 Fu-Bin Liu  4 Yuan-Xuan Cai  1 Rui-Hong Chen  5 Jin Han  6
Affiliations
  • 1. Department of Thyroid and Breast Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, Guangdong Province, China.
  • 2. Department of Paediatric Surgery Clinic, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, Guangdong Province, China.
  • 3. Department of Gynecologic Oncology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, Guangdong Province, China.
  • 4. The Third Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou, 510006, Guangdong Province, China.
  • 5. Department of Clinical Immunology, Institute of Clinical Laboratory Medicine, Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Guangdong Medical University, Dongguan, 523000, Guangdong Province, China. [email protected].
  • 6. Prenatal Diagnosis Center, Guangzhou Women and Children's Medical Center,, Guangzhou Medical University, Guangzhou, 510623, Guangdong Province, China. [email protected].
  • # Contributed equally.
Abstract

This study evaluated the inhibitory effects of calceolarioside B, extracted from the traditional Chinese herb Mutong (Akebia quinata Thumb), on the SARS-CoV-2 Omicron BA.2 variant. Molecular docking and molecular dynamics simulations predicted the binding sites and interactions between calceolarioside B and the Omicron BA.2 spike (S) protein. Biolayer interferometry (BLI) and immunofluorescence assays validated its high-affinity binding. Pseudovirus entry assays assessed the inhibitory effects of calceolarioside B on viral entry into host cells, while enzyme-linked immunosorbent assay (ELISA) measured inflammatory cytokine levels. Flow cytometry was used to analyze its effects on macrophage phenotype switching. Results demonstrated that calceolarioside B could bind to the Omicron BA.2 S protein with high affinity, and significantly inhibited viral entry into host cells by interfering with the binding of angiotensin-converting enzyme 2 (ACE2) receptor and S protein. Additionally, calceolarioside B reduced IL(interleukin)-6 expression levels and promoted the switch of macrophages from the pro-inflammatory M1 phenotype to the anti-inflammatory M2 phenotype. These findings suggest that calceolarioside B possesses Antiviral and immunomodulatory effects, making it a potential dual-function inhibitor for the treatment of COVID-19.

Keywords
Calceolarioside B; Immunomodulation; Molecular docking; SARS-CoV-2 Omicron BA.2; Viral inhibition.
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